A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749002



Internal ID21386346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50560241..50561240hg38UCSC Ensembl
chr10:52320001..52321000hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431343
Supporting Variants
SamplesMDQ010
Known GenesSGMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749002
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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